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Journal Abstract Search

235 related items for PubMed ID: 8260719

  • 1. Cosmid clones from microdissected human chromosomal region 15q11-q13.
    Tohma T, Tamura T, Ohta T, Soejima H, Kubota T, Jinno Y, Tsukamoto K, Nakamura Y, Naritomi K, Niikawa N.
    Jpn J Hum Genet; 1993 Sep; 38(3):267-75. PubMed ID: 8260719
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  • 3. Isolation and FISH mapping of 80 cosmid clones on the short arm of human chromosome 3.
    Haas M, Aburatani H, Stanton VP, Bhatt M, Housman D, Ward DC.
    Genomics; 1993 Apr; 16(1):90-6. PubMed ID: 8486389
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  • 9. Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish.
    Engelen JJ, Loots WJ, Albrechts JC, Schrander-Stumpel CT, Dirckx R, Smeets HJ, Hamers AJ, Geraedts JP.
    Genet Couns; 1999 Apr; 10(2):123-32. PubMed ID: 10422004
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  • 10. Isolation of region-specific cosmids by hybridization with microdissection clones from human chromosome 10q11.1-q21.1.
    Karakawa K, Takami K, Nakamura T, Jones C, Fujita S, Ohta T, Jinno Y, Niikawa N, Inazawa J, Ariyama T.
    Genomics; 1993 Aug; 17(2):449-55. PubMed ID: 8104874
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  • 11. Sequence tagged sites of microclones obtained by microdissection of a human chromosomal region 11q23 and isolation of yeast artificial chromosomes.
    Seki N, Yamauchi M, Saito T, Harada Y, Hori T.
    Jpn J Hum Genet; 1994 Jun; 39(2):249-54. PubMed ID: 8086642
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  • 12. [Application of the chromosome sorting technique to the human genome analysis].
    Minoshima S, Shimizu N.
    Nihon Rinsho; 1993 Sep; 51(9):2234-9. PubMed ID: 8411695
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  • 13. Characterization of a DNA sequence family in the Prader-Willi/Angelman syndrome chromosome region in 15q11-q13.
    Dittrich B, Knoblauch H, Buiting K, Horsthemke B.
    Genomics; 1993 Apr; 16(1):269-71. PubMed ID: 8486372
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  • 19. Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndrome.
    Delach JA, Rosengren SS, Kaplan L, Greenstein RM, Cassidy SB, Benn PA.
    Am J Med Genet; 1994 Aug 01; 52(1):85-91. PubMed ID: 7977469
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